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162  Autoimmune and Immune‐Mediated Skin Diseases  1427

               diagnostic value. Histopathology reveals interface vacu-  Initial lesions develop on haired skin and include ery-
  VetBooks.ir  olation and basal cell apoptosis.                  thematous macules and patches that progress to turgid
                 Clinical differential diagnoses include severe erythema
                                                                  vesicles. The lesions evolve to ulcers and crusts. Lesions
               multiforme, systemic lupus erythematosus, pemphigus
                                                                  spared and mucosa is less frequently affected than in
                 vulgaris, severe dermatomyositis, and bullous pemphigoid.  are not pruritic but can be painful. Pawpads are generally
                 Treatment involves immunosuppression using gluco-  mucous membrane pemphigoid.
               corticoids combined with azathioprine or ciclosporin.   Diagnosis is based on the dermatohistopathologic
               Pentoxifylline, vitamin E, topical glucocorticoids, or   findings of skin biopsy and immunofluorescence or
               hydroxychloroquine can be used as adjunctive therapy   immunohistochemistry. Refer to the subepidermal
               (see Table 162.1). Sun avoidance is potentially important     blistering diseases introduction for details about biopsy
               because sun exposure may be part of the disease patho-  technique and special testing. Histopathology reveals
               genesis. Topical and/or oral antibiotics along with  general   subepidermal bullae.
               wound care should also be instituted. Complications may   Clinical differential diagnoses include EBA (although
               include  secondary  pyoderma  and  even  septicemia.   EBA typically features footpad involvement), pemphigus
               Prognosis is generally good.                       variants, VCLE, and mucous membrane pemphigoid.
                                                                  The presence of nonmucosal involvement is   more
                                                                    suggestive of BP than mucous membrane pemphigoid.
                 Autoimmune Subepidermal                           Treatment involves topical glucocorticoids, oral gluco-
               Blistering Diseases                                corticoids, tetracycline with niacinamide, and/or azathio-
                                                                  prine (see Table 162.1). Complications include pyoderma.
               This group of diseases is autoimmune in nature and charac-  Spontaneous remission has been reported although it
               terized by vesicle formation on various parts of the body. The   should be anticipated that life‐long therapy could be
               diagnosis is based on signalment, physical examination, his-  necessary.
               topathology, and response to therapy. Immunohistochemistry
               or immunofluorescence is also sometimes required to   Epidermolysis Bullosa Acquisita
                 differentiate among the blistering diseases.
                 Bulla or vesicles should be sampled via wedge biopsy   Epidermolysis bullosa acquisita is an autoimmune vesic-
               for diagnostic purposes. If only erosions and ulcers are   ulobullous disease that affects mostly young adult dogs.
               present, the clinician should obtain a wedge biopsy   Great Danes and male dogs are overrepresented.
               encompassing both margins of an erosive lesion. It is   Initial lesions include patchy erythema and vesicles of
               important to include epidermis in the sample. A biopsy   the face, oral cavity, concave pinna, axilla, and groin
               that includes only dermis (e.g., center of an erosion or   (Figure 162.5).
               ulcer) will yield minimal diagnostic information. Samples   Vesicles may be hemorrhagic. Areas of friction tend to
               should be submitted to an experienced dermatohisto-  have the most obvious lesions. The groin and axilla
               pathologist to increase the chances of obtaining a defini-  develop erosions quickly. The oral mucosa and footpads
               tive diagnosis. Response to therapy and lesion appearance   usually feature extensive sloughing. Affected individuals
               can also guide the diagnosis. Bullous pemphigoid and
               mucous membrane pemphigoid are fairly glucocorticoid
               responsive, while epidermolysis bullosa acquisita (EBA)
               is more glucocorticoid resistant.
                 The mucous membranes are predominantly affected
               in mucous membrane pemphigoid. Areas of friction and
               trauma  (i.e., footpads) are predominantly affected  in
               EBA. Vesicular cutaneous lupus erythematosus (dis-
               cussed  above)  features  extensive  abdominal  erosions.
               Bullous pemphigoid and EBA generally feature tense
               vesicles, while the vesicles of vesicular cutaneous lupus
               erythematosus are more flaccid.


               Bullous Pemphigoid
               Bullous pemphigoid (BP) is an autoimmune vesiculobul-  Figure 162.5  One‐year‐old Great Dane with epidermolysis bullosa
               lous disease that more often affects middle‐aged dogs.   acquisita. Note the ulcers on the buccal mucosa and vesiculation
               Breed and sex predilections have not been identified.  at the lower lip margin. Source: Courtesy of Sandra Koch.
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